Recent Progress on Coking and Regeneration in the Methanol-to -Olefins (MTO) Reaction

doi:10.6023/A26030072

Acta Chimica Sinica

Review

甲醇制烯烃（MTO）反应积炭演化和再生研究进展

张琴^a,b,c,#, 陈祎瑶^a,b,c,#, 牛晶^a,b, 郅玉春^a,b,c,*, 徐舒涛^a,b,c,*, 魏迎旭^a,b,c, 刘中民^a,b,c

^a中国科学院大连化学物理研究所低碳催化技术国家工程研究中心辽宁大连 116023;
^b中国科学院大连化学物理研究所能源催化转化全国重点实验室辽宁大连 116023;
^c中国科学院大学北京 100049

投稿日期:2026-03-12
作者简介:张琴,中国科学院大学大连化学物理研究生。本科毕业于宁夏大学化学化工学院。主要研究方向为甲醇和烃类耦合反应机理研究。陈祎瑶,中国科学院大连化学物理研究所博士生。本科毕业于浙江工业大学化工学院。主要研究方向为甲醇制烯烃积炭失活机理研究。牛晶,中国科学院大连化学物理研究所博士后。2023年博士毕业于兰州大学化学化工学院,毕业后至大连化学物理研究所从事博士后研究。研究方向为通过先进固体核磁共振技术阐明分子筛催化醇类及其耦合反应机制。郅玉春,中国科学院大连化学物理研究所研究员。2007年本科毕业于山东大学材料学院,2010年硕士毕业于山东大学晶体材料国家重点实验室,2015年博士毕业于德国慕尼黑工业大学,毕业后在大连化学物理研究所工作,主要研究方向围绕甲醇制烯烃过程,从事甲醇转化机理研究、分子筛积炭失活机制及产物选择性调控机理研究。徐舒涛,中国科学院大连化学物理研究所研究员,优青。2004年本科毕业于复旦大学化学系,2010年博士毕业于中国科学院大连化学物理研究所。现为大连化物所低碳催化技术国家工程研究中心科研骨干。2016年获第16届国际催化大会青年科学家奖（Young Scientist Prize）,2023年获中国化学会分子筛青年奖,2025年获辽宁省自然科学一等奖（2024年度,3/5）。主要研究方向为原位固体核磁谱学技术在分子筛催化中的应用。魏迎旭,中国科学院大连化学物理研究所研究员。1993年学士毕业于上海交通大学应用化学系,2001年博士毕业于中科院大连化学物理研究所物理化学专业,毕业后在大连化学物理研究所工作,期间于2003-2004年赴比利时Namur大学进行博士后研究。现为低碳催化技术国家工程研究中心研究员,催化反应机理和新反应探索研究组组长。从事分子筛催化、甲醇制烯烃、烷烃转化及二氧化碳耦合烷烃转化制高值化学品的基础和应用研究。入选科技部创新人才推进计划中青年科技创新领军人才、大连化学物理研究所首席研究员、张大煜优秀学者等,获辽宁省自然科学一等奖（2024年度,1/5）。刘中民,中国工程院院士,中国科学院大连化学物理研究所所长、低碳催化技术国家工程研究中心主任、国家能源低碳催化与工程研发中心主任。1983年学士毕业于郑州大学,1986年硕士毕业于中科院大连化物所,1990年在中科院大连化物所获得博士学位,1996年3月至1996年10月,在法国科研中心CNRS418(Montpellier)开展博士后工作。刘中民院士长期从事应用催化研究,作为技术总负责人合作完成了多项创新成果并实现产业化。完成了世界首次甲醇制烯烃（DMTO）技术工业性试验及首次工业化;完成了世界首套10万吨/年煤基乙醇（DMTE）工业示范项目,引领了我国新兴煤制大宗化学品和清洁燃料产业的发展。
基金资助:
项目受国家自然科学基金(No. U25A20555; 22241801; U25D9013; 22288101; 22372164),辽宁国际联合实验室项目(2024JH2/102100005)资助

Recent Progress on Coking and Regeneration in the Methanol-to -Olefins (MTO) Reaction

Zhang Qin^a,b,c,#, Chen Yiyao^a,b,c,#, Niu Jing^a,b, Zhi Yuchun^a,b,c,*, Xu Shutao^a,b,c,*, Wei Yingxu^a,b,c, Liu Zhongmin^a,b,c

^aNational Engineering Research Center of Lower-Carbon Catalysis Technology, Dalian Institute of Chemical Physics, Chinese Academy of Sciences, Dalian 116023, Liaoning, China;
^bState Key Laboratory of Catalysis, Dalian Institute of Chemical Physics, Chinese Academy of Sciences, Dalian 116023, Liaoning, China;
^cUniversity of Chinese Academy of Sciences, Beijing 100049, China.

Received:2026-03-12
Contact: ^*E-mail: xushutao@dicp.ac.cn; yuchunzhi@dicp.ac.cn
About author:^#Zhang qin and Chen Yiyao contribute equally to this work.
Supported by:
National Natural Science Foundation of China (No. U25A20555; 22241801; U25D9013; 22288101; 22372164), Liaoning International Joint Laboratory Project (2024JH2/102100005).

The methanol-to-olefins (MTO) technology, as a non-petroleum-dependent low-carbon olefin production route, has successfully broken through the rely of traditional olefin industries on petroleum resources. It has become an important way to obtain key chemical raw materials such as ethylene and propylene, and has achieved large-scale industrial application. During the MTO reaction process, SAPO-34 and HZSM-5 molecular sieves are the most representative catalysts. However, in the actual reaction process, they are prone to deactivation due to coke deposition, which affects the olefin yield and selectivity, and restricts the stable operation and long-term operation of the device. This review systematically summarizes the research progress of the MTO reaction process and its core catalyst system, with a focus on the formation and evolution mechanism of coke species. By deeply analyzing the structure, composition, and dynamic change characteristics of coke it reveals that coke deposition is not a single component but a continuous mixture that gradually evolves from soluble aromatic hydrocarbons to insoluble fused-ring aromatic hydrocarbons. Based on the systematic analysis of the coke deposition behavior of SAPO-34 and HZSM-5 molecular sieves, the "cage-passing growth" mechanism for SAPO-34 molecular sieves and the "channel intersection-passing growth" mechanism for HZSM-5 molecular sieves are proposed, revealing the essential similarity in the coke evolution paths. On this basis, the influence of coke deposition on catalyst activity, stability, and olefin selectivity are further summarized, and the main progress in regulatory strategies is systematically summarized from two dimensions: delaying catalyst deactivation and optimizing the regeneration process. Finally, the development direction of the existing technology system is prospected to provide a reference for the development of efficient anti-coke deposition catalysts and the continuous improvement of the MTO process.

Key words: MTO, coke, SAPO-34, HZSM-5, catalyst deactivation, catalyst regeneration

Cite this article

Zhang Qin, Chen Yiyao, Niu Jing, Zhi Yuchun, Xu Shutao, Wei Yingxu, Liu Zhongmin. Recent Progress on Coking and Regeneration in the Methanol-to -Olefins (MTO) Reaction[J]. Acta Chimica Sinica, doi: 10.6023/A26030072.

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甲醇制烯烃（MTO）反应积炭演化和再生研究进展

Recent Progress on Coking and Regeneration in the Methanol-to -Olefins (MTO) Reaction

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